Prakash C

Highly Motivated well versed with all facets of Supply Chain Management includes Demand & Supply Planning, Production Planning, Production Scheduling, Material Management, Warehousing & Logistics, Inventory Management, Packaging Material Procurement, CMO Strategy & Operations, New Product Launch, Cost Optimization Projects, Site Transfer Project Management and Managing Change Management IT Skills: SAP ECC, SAP APO, MPS Planning and MS Office

• Service Level of 95% for Priority Molecule
• SCM KPI's set up
• Improved SKU level Availability for Business at distribution centers
• Reduction in Back Order
• Savings in Transportation by Shifting products from Air to Sea
• Cost Savings in packaging material procurement by developing local supplier for bottles and foils
• SCM Module Implementation (SNP & PPDS)
• Supply Chain Department Set up in Apotex India

• Supply chain planner accountable for complete raw/packaging material Planning for 3 billion yearly solid oral dosages, focused on minimizing back orders and maximizing line fill rate.
• Proficient SAP ECC & SAP APO operator, familiar with material management and stock overview, along with production planning & supply planning.
• Efficient material planning and management skills to enable uninterrupted manufacturing and increased volumes.
• Excellence in stakeholder management, process improvements, problem solving & analytical skills.
• Focusing on compliance, excellent Interpersonal relationship skills, optimum customer service.
• SAP MM (Materials Management) role in a manufacturer's supply chain
• Initiation of Purchase Request, creation of Bill of Material (Manufacturing and Packing), and all production related SAP transaction.
• Initiated and qualified SAP Track and Trace in packing line.
• Initiation and driving the Change control for PVR recommendation, APQR recommendation, new production introduction, MFR revision, CAPA and Audit compliance.
• Overall accountability to ensure and maintain RM readiness to execute monthly manufacturing plans.
• Initiation and driving the Deviation activities related to manufacturing and packing.
• Handling of “Track wise” operations for all BMR, BPR and CCR activities (Doc data & QMS).
• Preparing SOPs, Format, Operating Instructions and Standard Cleaning procedures for Equipments and online execution of all related documents.
• Planning & monitoring the work schedules for weekly & monthly.
• Conduct CFT meetings related to major CCR, revision in SOP and Audit compliance.
• Controlling of GMP documents and records.
• Supported in all time audit readiness.

• CANADA
• USFDA
• MHRA
• TGA